期刊
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
卷 46, 期 9, 页码 3851-3857出版社
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2011.05.053
关键词
Crystal structure; Bicopper(II) complexes; Oxamido-bridge; Cytotoxicity; DNA interaction
资金
- Natural Science Foundation of China [21071133]
- Natural Science Foundation of Qingdao City [09-1-3-73-jch]
- Program for Changjiang Scholars and Innovative Research Teamin University [IRT0944]
A novel dissymmetrical N,N'-bis(substituted)oxamide ligand, N-(2-aminopropyl)-N'-(2-oxido- phenyl) oxamide (H(3)apopoxd) (L), and its three bicopper(II) complexes, [Cu-2(apopoxd)(bpy)]- (ClO4)center dot H2O (1), [Cu-2(apopoxd)(dabt)](ClO4)center dot 2H(2)O (2), and [Cu-2(apopoxd)(phen)(2)](ClO4) (3) (bpy = 2,2'-bipyridine; dabt = 2,2'-diamino-4,4'-bithiazole; phen = 1,10-phenanthroline) have been synthesized and characterized. The crystal structures of the three bicopper(II) complexes have been determined by X-ray single-crystal diffraction. In complexes 1 and 2, the cis-apopoxd(3-) ligands bridge two copper(II) ions in square-planar geometries with the corresponding separations of 5.1868(3) and 5.2016(4) angstrom, respectively. While in complex 3, the apopoxd(3-) ligand adopting a trans conformation bridges the two copper(II) ions in distorted square-pyramid environments with a Cu center dot center dot center dot Cu distance of 5.2508(7) angstrom. The anticancer activities and DNA-binding properties of L and the three complexes were investigated. (C) 2011 Elsevier Masson SAS. All rights reserved.
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